• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 > 
 
18 records meeting your search criteria returned- Product Code: DTK Patient Problem: Calcium Deposits/Calcification Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION UNKNOWN VENA CAVA FILTER 08/25/2020
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 04/01/2020
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 12/31/2019
CORDIS CASHEL 466P306X 12/30/2019
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 12/17/2019
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 06/04/2019
CORDIS CASHEL 466FXXXX 03/11/2019
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 02/25/2019
CORDIS CASHEL 466FXXXX 01/30/2019
CORDIS CASHEL UNKNOWN VENA CAVA FILTER 09/17/2018
-
-